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T Ikeuchi

Showing results (291-300 of 303) with videos related to

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Neuropathology and Applied Neurobiology|October 11, 2019
Morphological characterisation of glial and neuronal tau pathology in globular glial tauopathy (Types II and III)H Tanaka, Y Toyoshima, S Kawakatsu, et al.
The Annals of Thoracic Surgery|January 5, 2000
Evaluation of the accuracy of preoperative staging in thoracic esophageal cancerT Nishimaki, O Tanaka, N Ando, et al.
AJNR. American Journal of Neuroradiology|September 17, 2016
Diagnostic Value of Brain Calcifications in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented GliaT Konno, D F Broderick, N Mezaki, et al.
Neurology|December 31, 1997
Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy. Influence of CAG repeat size on MRI findingsR Koide, O Onodera, T Ikeuchi, et al.
Genomics|May 23, 1998
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17qT Ikeuchi, K Sanpei, H Takano, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|June 26, 2008
[The clinical-genealogic and molecular-genetic characteristics of oculopharyngeal muscular dystrophy in the Republic of Sakha (Yakutia)]N R Maksimova, I A Nikolaeva, M N Korotkov, et al.
American Journal of Human Genetics|August 1, 1997
Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1K Ishikawa, H Tanaka, M Saito, et al.
Nature Genetics|February 14, 1998
Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretchS Igarashi, R Koide, T Shimohata, et al.
American Journal of Human Genetics|October 3, 1998
Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populationsH Takano, G Cancel, T Ikeuchi, et al.
Human Molecular Genetics|January 15, 1999
Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patientsT Sato, M Oyake, K Nakamura, et al.
Pageof 31

Showing results (291-300 of 303) with videos related to

Sort By:
Pageof 31
Neuropathology and Applied Neurobiology|October 11, 2019
Morphological characterisation of glial and neuronal tau pathology in globular glial tauopathy (Types II and III)H Tanaka, Y Toyoshima, S Kawakatsu, et al.
The Annals of Thoracic Surgery|January 5, 2000
Evaluation of the accuracy of preoperative staging in thoracic esophageal cancerT Nishimaki, O Tanaka, N Ando, et al.
AJNR. American Journal of Neuroradiology|September 17, 2016
Diagnostic Value of Brain Calcifications in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented GliaT Konno, D F Broderick, N Mezaki, et al.
Neurology|December 31, 1997
Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy. Influence of CAG repeat size on MRI findingsR Koide, O Onodera, T Ikeuchi, et al.
Genomics|May 23, 1998
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17qT Ikeuchi, K Sanpei, H Takano, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|June 26, 2008
[The clinical-genealogic and molecular-genetic characteristics of oculopharyngeal muscular dystrophy in the Republic of Sakha (Yakutia)]N R Maksimova, I A Nikolaeva, M N Korotkov, et al.
American Journal of Human Genetics|August 1, 1997
Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1K Ishikawa, H Tanaka, M Saito, et al.
Nature Genetics|February 14, 1998
Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretchS Igarashi, R Koide, T Shimohata, et al.
American Journal of Human Genetics|October 3, 1998
Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populationsH Takano, G Cancel, T Ikeuchi, et al.
Human Molecular Genetics|January 15, 1999
Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patientsT Sato, M Oyake, K Nakamura, et al.
Pageof 31